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Chemical Structure| 857650-89-6 Chemical Structure| 857650-89-6

Structure of 857650-89-6

Chemical Structure| 857650-89-6

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Product Details of [ 857650-89-6 ]

CAS No. :857650-89-6
Formula : C19H24F3N3O4
M.W : 415.41
SMILES Code : O=C(OC(C)(C)C)N[C@@H]1CN(C(CNC(C2=CC=CC(C(F)(F)F)=C2)=O)=O)CC1

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Application In Synthesis of [ 857650-89-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 857650-89-6 ]

[ 857650-89-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17794-48-8 ]
  • [ 122536-76-9 ]
  • [ 857650-89-6 ]
YieldReaction ConditionsOperation in experiment
96% With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In DMF (N,N-dimethyl-formamide); at 0 - 20℃; tert-Butyl [(3S)-1-([3-(Trifluoromethyl)benzoyl]amino}acetyl)pyrrolidin-3-yl]carbamate. To a solution of the carboxylic acid (2.7 g, 11 mmol) from step A and tert-butyl (3S)-pyrrolidin-3-ylcarbamate (2.0 g, 11 mmol) in DMF (30 mL) cooled in an ice bath was added BOP (5 g, 11 mmol) followed by triethylamine (3 mL, 22 mmol). The mixture was allowed to warm to temperature and stirred overnight. Ethyl acetate (150 mL) was added. The resulting solution was washed with NaHCO3 and brine each three times, dried over MgSO4 and concentrated. Chromatography on silica gel eluting with EtOAc provided 4.4 g (96%) of the desired product. MS (M-Boc+H)+ 316.
96% With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20℃;cooling with ice; Step BBocHN'tert-Butyl [(3S)-1 -([3-(Trifluoromethyl)benzoyl]amino}acetyl)pyrrolidin-3-yl]carbamate. To a solution of the carboxylic acid (2.7 g, 1 1 mmol) from step A and tert-butyl (3S)-pyrrolidin-3-ylcarbamate (2.0 g, 1 1 mmol) in DMF (30 mL) cooled in an ice bath was added BOP (5 g, 1 1 mmol) followed by triethylamine (3 mL, 22 mmol). The mixture was allowed to warm to temperature and stirred overnight. Ethyl acetate (150 mL) was added. The resulting solution was washed with NaHC03 and brine each three times, dried over MgS04 and concentrated. Chromatography on silica gel eluting with EtOAc provided 4.4 g (96%) of the desired product. MS (M-Boc+H)+ 316.
 

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